Name: cathepsin L |
Aliases:
Cat L,
RIKEN cDNA 1190035F06 gene,
major excreted protein,
nackt,
1190035F06Rik,
furless,
fs,
MEP,
nkt
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Description: PHENOTYPE: Homozygotes for mutant alleles may show partial or complete hair-loss, skin defects, impaired T cell maturation, dilated cardiomyopathy, and high postnatal mortality. Mutant males for some alleles show both normal and atrophic seminiferous tubules and reduced sperm production. [provided by MGI curators] |
Crossreferences:
MGI:88564,
UniProtKB:A0A1Y7VNQ4,
UniProtKB:Q3UHZ4,
UniProtKB:Q3TNC8,
UniProtKB:Q3TVJ1,
UniProtKB:A0A1Y7VP49,
UniProtKB:P06797,
UniProtKB:Q9D0C0,
UniProtKB:Q3TT75,
UniProtKB:Q3UWH6,
ENSEMBL:ENSMUSG00000021477,
NCBI_Gene:13039,
UniProtKB:Q543M3,
UniProtKB:Q6LAF5,
UniProtKB:A0A1Y7VNM3,
UniProtKB:Q3U5U9,
UniProtKB:A0A1Y7VJC1
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This information is supplied by the AllianceGenome.org API. |